Calmodulin and CaMKII as molecular switches for cardiac ion channels

Cardiovasc Res. 2007 Mar 1;73(4):641-7. doi: 10.1016/j.cardiores.2006.10.019. Epub 2006 Nov 10.

Abstract

Because changes in intracellular Ca(2+) concentration are the final signals of electrical activity in excitable cells, many mechanisms have evolved to regulate Ca(2+) influx. Among the most important are those pathways that directly regulate the ion channels responsible for regulating and generating the Ca(2+) influx signal. Recent work has demonstrated that the Ca(2+) binding protein calmodulin (CaM) and the Ca(2+)/CaM-sensitive kinase CaMKII are important modulators of cardiac ion channels. Thus, Ca(2+) participates in feedback modulation to control electrical activity. This review highlights various mechanisms by which CaM and CaMKII regulate cardiovascular ion channel activity and presents a novel model for CaMKII regulation of Ca(V)1.2 Ca(2+) channel function.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Animals
  • Calcium Channels, L-Type / metabolism
  • Calcium-Calmodulin-Dependent Protein Kinase Type 2
  • Calcium-Calmodulin-Dependent Protein Kinases / metabolism*
  • Calmodulin / metabolism*
  • Humans
  • Ion Channel Gating / physiology*
  • Ion Channels / metabolism*
  • Models, Molecular
  • Potassium Channels, Calcium-Activated / metabolism
  • Ryanodine Receptor Calcium Release Channel / metabolism

Substances

  • Calcium Channels, L-Type
  • Calmodulin
  • Ion Channels
  • Potassium Channels, Calcium-Activated
  • Ryanodine Receptor Calcium Release Channel
  • Calcium-Calmodulin-Dependent Protein Kinase Type 2
  • Calcium-Calmodulin-Dependent Protein Kinases